DIFFERENTIAL SECRETION OF FOLLICLE-STIMULATING-HORMONE AND LUTEINIZING-HORMONE FROM OVINE PITUITARY-CELLS FOLLOWING ACTIVATION OF PROTEIN-KINASE-A, PROTEIN-KINASE-C, OR INCREASED INTRACELLULAR CALCIUM
Jp. Kile et Tm. Nett, DIFFERENTIAL SECRETION OF FOLLICLE-STIMULATING-HORMONE AND LUTEINIZING-HORMONE FROM OVINE PITUITARY-CELLS FOLLOWING ACTIVATION OF PROTEIN-KINASE-A, PROTEIN-KINASE-C, OR INCREASED INTRACELLULAR CALCIUM, Biology of reproduction, 50(1), 1994, pp. 49-54
A higher dose of GnRH is required to stimulate release of FSH than of
LH, both in vivo and in vitro. Therefore, we tested the hypothesis tha
t secretion of FSH may be mediated via a second messenger pathway diff
erent from the one that modulates secretion of LH. Pituitary cells fro
m intact ewes were cultured in suspension in DMEM plus 1O% wether seru
m. After 18 h, cell were washed and challenged for 2 h with agents cap
able of activating protein kinase A (dibutyryl cAMP), protein kinase C
(phorbol 12-myristate 13-acetate; PMA), or increasing intracellular c
alcium (the calcium ionophore A23187). GnRH (0.01-10 nM) and PMA (0.2-
20 nM) stimulated dose-dependent increases in secretion of LH. FSH sec
retion also was stimulated by GnRH and PMA; however, the percentage of
total cellular FSH released was lower (p < 0.05) than the percentage
of total cellular LH released. Dibutyryl cAMP (10 mM) induced a modest
release (p < 0.05) of both LH and FSH. A23187 (1-10 mu M) stimulated
secretion of LH in a dose-dependent manner but did not influence secre
tion of FSH; however, GnRH- and PMA-induced secretion of FSH required
the presence of intracellular calcium. On the basis of the results of
this study, we suggest that secretion of FSH is less than secretion of
LH following direct activation of these second messenger systems. Fur
thermore, we suggest that in contrast to the situation for LH, increas
ed intracellular calcium is not the primary stimulus for inducing secr
etion of FSH.